BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756355056·SHOULDER PACK

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112335·SURG-I-BAND LIME GREEN

    BABI PLUS INFANT NASAL CANNULA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AFOCUS ELECTROPYSIOLOGY CATHETER SYSTEM, MODELS 81550, 81567, 81568, 81569

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 17, 2013

    EEA 31MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GDW·November 24, 2010

    UNKNOWN REJUVENATE STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·January 8, 2013

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 2, 2014

    MICRUSFRAME10 5MM X 9.7CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·April 23, 2021